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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757267Generated: October 25, 2026

Hydrochloric Acid → (E)-diethylphosphono-(6,6-dimethyl-2-hepten-4-ynyl)acetic acid ethyl ester

https://huagongshe.com/reaction/1757267

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethyl phosphonoacetateHCID 13345—
ReactantSodium hydrideHCID 24758—
Reactant2-Hepten-4-yne, 1-bromo-6,6-dimethyl-HCID 11074428—
SolventEthanolHCID 702—
Product(E)-diethylphosphono-(6,6-dimethyl-2-hepten-4-ynyl)acetic acid ethyl esterHCID 8674893466.8%

Reaction Steps

3.34 g of diethylphosphonoacetic acid ethyl ester is dissolved in 40 ml of ethanol, 594 mg of 60% oily sodium hydride is added under ice cooling and stirring, and ethanol solution (10 ml) of 600 mg of (E)-6,6-dimethyl-2-hepten-4-ynyl bromide is added dropwise, and the mixture is stirred for 5 hours. The reaction solution is neutralized with 1N hydrochloric acid and then concentrated under reduced pressure, the residue is dissolved in a mixture of water with ethyl acetate, the organic layer is taken and post-treated in a conventional manner, and the product is purified by silica gel column chromatography [Wako gel C-200, 140 g; hexane/ethyl acetate=3/1→1/1] to obtain 686 mg of (E)-diethylphosphono-(6,6-dimethyl-2-hepten-4-ynyl)acetic acid ethyl ester as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05444084
Source datasetuspto-grants-1995_08
ORD IDord-eadec35c878543cebd2d8a64493f2f8e
Source noteuspto-grants-1995_08